|
ENST00000457416.7:c.1087+1240del
MANE Plus Clinical
|
ENSP00000410294.2:n.1087+1240del
|
|
|
ENST00000351936.11:c.961del
|
ENSP00000309878.10:p.Asp321ThrfsTer12
|
|
|
ENST00000638709.2:c.-210del
|
ENSP00000491912.2:n.-210del
|
|
|
ENST00000682296.1:n.309del
|
|
|
|
ENST00000682400.1:n.616del
|
|
|
|
ENST00000682550.1:c.616del
|
ENSP00000507633.1:p.Asp206ThrfsTer12
|
|
|
ENST00000682772.1:c.-210del
|
ENSP00000506848.1:n.-210del
|
|
|
ENST00000683211.1:c.961del
|
ENSP00000508257.1:p.Asp321ThrfsTer12
|
|
|
ENST00000683250.1:c.404-13501del
|
ENSP00000506847.1:n.404-13501del
|
|
|
ENST00000683418.1:n.3308del
|
|
|
|
ENST00000683678.1:n.961del
|
|
|
|
ENST00000684153.1:c.616del
|
ENSP00000506937.1:p.Asp206ThrfsTer12
|
|
|
ENST00000358487.10:c.961del
MANE Select
|
ENSP00000351276.6:p.Asp321ThrfsTer12
|
|
|
ENST00000336553.10:c.694del
|
ENSP00000337665.6:p.Asp232ThrfsTer12
|
|
|
ENST00000346997.6:c.961del
|
ENSP00000263451.5:p.Asp321ThrfsTer12
|
|
|
ENST00000351936.10:c.967del
|
ENSP00000309878.9:p.Asp323ThrfsTer12
|
|
|
ENST00000356226.8:c.616del
|
ENSP00000348559.4:p.Asp206ThrfsTer12
|
|
|
ENST00000357555.9:c.694del
|
ENSP00000350166.5:p.Asp232ThrfsTer12
|
|
|
ENST00000358487.9:c.961del
|
ENSP00000351276.5:p.Asp321ThrfsTer12
|
|
|
ENST00000360144.7:c.820+1240del
|
ENSP00000353262.3:n.820+1240del
|
|
|
ENST00000369056.5:c.1087+1240del
|
ENSP00000358052.1:n.1087+1240del
|
|
|
ENST00000369058.7:c.1087+1240del
|
ENSP00000358054.3:n.1087+1240del
|
|
|
ENST00000369059.5:c.742+1240del
|
ENSP00000358055.1:n.742+1240del
|
|
|
ENST00000369060.8:c.939+2537del
|
ENSP00000358056.4:n.939+2537del
|
|
|
ENST00000369061.8:c.749-2123del
|
ENSP00000358057.4:n.749-2123del
|
|
|
ENST00000457416.6:c.1087+1240del
|
ENSP00000410294.2:n.1087+1240del
|
|
|
ENST00000463870.5:n.170del
|
|
|
|
ENST00000478859.5:c.277del
|
ENSP00000474011.1:p.Asp93ThrfsTer12
|
|
|
ENST00000490349.5:n.1370del
|
|
|
|
ENST00000604236.5:c.*8del
|
ENSP00000474109.1:n.*8del
|
|
|
ENST00000613048.4:c.694del
|
ENSP00000484154.1:p.Asp232ThrfsTer12
|
|
|
NM_000141.4:c.961del
|
NP_000132.3:p.Asp321ThrfsTer12
|
|
|
NM_001144913.1:c.1087+1240del
|
NP_001138385.1:n.1087+1240del
|
|
|
NM_001144914.1:c.749-2123del
|
NP_001138386.1:n.749-2123del
|
|
|
NM_001144915.1:c.694del
|
NP_001138387.1:p.Asp232ThrfsTer12
|
|
|
NM_001144916.1:c.616del
|
NP_001138388.1:p.Asp206ThrfsTer12
|
|
|
NM_001144917.1:c.939+2537del
|
NP_001138389.1:n.939+2537del
|
|
|
NM_001144918.1:c.616del
|
NP_001138390.1:p.Asp206ThrfsTer12
|
|
|
NM_001144919.1:c.820+1240del
|
NP_001138391.1:n.820+1240del
|
|
|
NM_022970.3:c.1087+1240del
|
NP_075259.4:n.1087+1240del
|
|
|
NM_023029.2:c.694del
|
NP_075418.1:p.Asp232ThrfsTer12
|
|
|
NR_073009.1:n.1411del
|
|
|
|
XM_006717708.2:c.1144+1240del
|
XP_006717771.1:n.1144+1240del
|
|
|
XM_006717709.2:c.1018del
|
XP_006717772.1:p.Asp340ThrfsTer12
|
|
|
XM_006717710.2:c.1144+1240del
|
XP_006717773.1:n.1144+1240del
|
|
|
XM_006717711.2:c.877+1240del
|
XP_006717774.1:n.877+1240del
|
|
|
XM_006717712.2:c.799+1240del
|
XP_006717775.1:n.799+1240del
|
|
|
XM_006717713.2:c.1018del
|
XP_006717776.1:p.Asp340ThrfsTer12
|
|
|
XM_011539510.1:c.277del
|
XP_011537812.1:p.Asp93ThrfsTer12
|
|
|
NM_001320654.1:c.277del
|
NP_001307583.1:p.Asp93ThrfsTer12
|
|
|
NM_001320658.1:c.961del
|
NP_001307587.1:p.Asp321ThrfsTer12
|
|
|
XM_006717708.3:c.1144+1240del
|
XP_006717771.1:n.1144+1240del
|
|
|
XM_006717710.4:c.1144+1240del
|
XP_006717773.1:n.1144+1240del
|
|
|
XM_017015920.2:c.1144+1240del
|
XP_016871409.1:n.1144+1240del
|
|
|
XM_017015921.2:c.1018del
|
XP_016871410.1:p.Asp340ThrfsTer12
|
|
|
XM_017015924.2:c.673del
|
XP_016871413.1:p.Asp225ThrfsTer12
|
|
|
XM_017015925.2:c.673del
|
XP_016871414.1:p.Asp225ThrfsTer12
|
|
|
XM_024447887.1:c.751del
|
XP_024303655.1:p.Asp251ThrfsTer12
|
|
|
XM_024447888.1:c.877+1240del
|
XP_024303656.1:n.877+1240del
|
|
|
XM_024447889.1:c.751del
|
XP_024303657.1:p.Asp251ThrfsTer12
|
|
|
XM_024447890.1:c.877+1240del
|
XP_024303658.1:n.877+1240del
|
|
|
XM_024447891.1:c.799+1240del
|
XP_024303659.1:n.799+1240del
|
|
|
XM_024447892.1:c.-210del
|
XP_024303660.1:n.-210del
|
|
|
NM_000141.5:c.961del
MANE Select
|
NP_000132.3:p.Asp321ThrfsTer12
|
|
|
NM_001144917.2:c.939+2537del
|
NP_001138389.1:n.939+2537del
|
|
|
NM_001144918.2:c.616del
|
NP_001138390.1:p.Asp206ThrfsTer12
|
|
|
NM_001144919.2:c.820+1240del
|
NP_001138391.1:n.820+1240del
|
|
|
NM_001320658.2:c.961del
|
NP_001307587.1:p.Asp321ThrfsTer12
|
|
|
NR_073009.2:n.1397del
|
|
|
|
NM_001144915.2:c.694del
|
NP_001138387.1:p.Asp232ThrfsTer12
|
|
|
NM_001144916.2:c.616del
|
NP_001138388.1:p.Asp206ThrfsTer12
|
|
|
NM_001320654.2:c.277del
|
NP_001307583.1:p.Asp93ThrfsTer12
|
|
